Canonical Allele Identifier: PA2829981458
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65229
ClinVar RCV Id: RCV000055449 RCV000166370 RCV000813618 RCV000518605 RCV003996481
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val1457Met
CA020558
NM_021055.3:c.4369G>A